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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Turn All System — 14 UDI-DI variants, MDR (Levabo ApS)

MD Atlas
Levabo ApS

Data from EUDAMED, last updated May 23, 2026

Turn All System

5711014turnallLB

14 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Levabo ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5711014turnallLB
Device name: Turn All System
Device model: Turn All
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 2026

Manufacturer & authorised representative

Manufacturer

Name: Levabo ApS
SRN: DK-MF-000014646
Country: Denmark
Email: ke@levabo.dk
Phone: +4540220333

Variants by status

UDI-DI variants

14 UDI-DI variants

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Applied filters

basicUdiUlid01KS0W6KRVG6R2J3844CA6SX9X

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

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7009805711014700989
7616705711014761676
7621005711014762109
7616805711014761683
7012605711014701269
7012405711014701245
7011405711014701146
7016105711014701610
7008205711014700828
7011205711014701122
7022505711014702259
7022605711014702266
7617205711014761720